A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14302045



Internal ID22274990
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:11856129..11860059hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg383931
Variant TypeOTHER copy number variation
Copy Number47
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3204514
Supporting Variants
SamplesNA19239
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14302045
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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